Canonical Allele Identifier: CA489741004

Gene: IVD

Linked Data

• MyVariant Identifiers: chr15:g.40703803T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411604T>G , CM000677.2:g.40411604T>G	GRCh38
NC_000015.9:g.40703803T>G , CM000677.1:g.40703803T>G	GRCh37
NC_000015.8:g.38491095T>G	NCBI36
NG_011986.1:g.11118T>G
NG_011986.2:g.11120T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.510T>G	ENSP00000417990.3:p.Pro170=
ENST00000487418.8:c.600T>G MANE Select	ENSP00000418397.3:p.Pro200=
ENST00000650656.1:c.519T>G	ENSP00000498731.1:p.Pro173=
ENST00000651168.1:c.609T>G	ENSP00000499074.1:p.Pro203=
ENST00000473112.6:c.359T>G
ENST00000479013.6:c.519T>G	ENSP00000417990.2:p.Pro173=
ENST00000481262.6:c.206T>G
ENST00000484250.1:n.223T>G
ENST00000487418.6:c.609T>G	ENSP00000418397.2:p.Pro203=
ENST00000558610.5:c.552T>G	ENSP00000453821.1:p.Pro184=
NM_001159508.1:c.519T>G	NP_001152980.1:p.Pro173=
NM_002225.3:c.609T>G	NP_002216.2:p.Pro203=
XM_005254350.2:c.609T>G	XP_005254407.1:p.Pro203=
XM_005254356.2:c.609T>G	XP_005254413.1:p.Pro203=
XM_006720491.2:c.552T>G	XP_006720554.1:p.Pro184=
XM_006720492.2:c.609T>G	XP_006720555.1:p.Pro203=
XM_006720493.2:c.609T>G	XP_006720556.1:p.Pro203=
XM_006720494.2:c.609T>G	XP_006720557.1:p.Pro203=
XM_006720495.2:c.609T>G	XP_006720558.1:p.Pro203=
XM_011521523.1:c.609T>G	XP_011519825.1:p.Pro203=
XM_011521524.1:c.609T>G	XP_011519826.1:p.Pro203=
XR_243097.3:n.609T>G
XR_243098.2:n.609T>G
XR_429453.2:n.710T>G
NM_001159508.2:c.510T>G	NP_001152980.2:p.Pro170=
NM_001354597.2:c.552T>G	NP_001341526.1:p.Pro184=
NM_001354598.2:c.600T>G	NP_001341527.2:p.Pro200=
NM_001354599.2:c.687T>G	NP_001341528.2:p.Pro229=
NM_001354600.2:c.687T>G	NP_001341529.2:p.Pro229=
NM_001354601.2:c.600T>G	NP_001341530.2:p.Pro200=
NM_002225.4:c.600T>G	NP_002216.3:p.Pro200=
NR_148925.1:n.1010T>G
XM_006720495.3:c.609T>G	XP_006720558.1:p.Pro203=
XM_017022149.1:c.696T>G	XP_016877638.1:p.Pro232=
XM_017022150.1:c.696T>G	XP_016877639.1:p.Pro232=
XM_017022153.1:c.696T>G	XP_016877642.1:p.Pro232=
XM_017022154.2:c.639T>G	XP_016877643.1:p.Pro213=
XM_017022155.2:c.696T>G	XP_016877644.1:p.Pro232=
XM_017022157.1:c.696T>G	XP_016877646.1:p.Pro232=
XM_017022158.2:c.696T>G	XP_016877647.1:p.Pro232=
XR_001751263.1:n.959T>G
XR_001751264.1:n.1000T>G
NM_001159508.3:c.510T>G	NP_001152980.2:p.Pro170=
NM_001354597.3:c.552T>G	NP_001341526.1:p.Pro184=
NM_001354598.3:c.600T>G	NP_001341527.2:p.Pro200=
NM_001354599.3:c.687T>G	NP_001341528.2:p.Pro229=
NM_001354600.3:c.687T>G	NP_001341529.2:p.Pro229=
NM_001354601.3:c.600T>G	NP_001341530.2:p.Pro200=
NM_002225.5:c.600T>G MANE Select	NP_002216.3:p.Pro200=
NR_148925.2:n.1012T>G